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RBM10 Modulates Apoptosis and Influences TNF-α Gene Expression
Author(s) -
Ke Wang,
Mackensey L. Bacon,
J Tessier,
Nina D. RintalaMaki,
Vanessa R. Tang,
Leslie C. Sutherland
Publication year - 2012
Publication title -
journal of cell death
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.419
H-Index - 15
ISSN - 1179-0660
DOI - 10.4137/jcd.s9073
Subject(s) - biology , apoptosis , gene knockdown , microbiology and biotechnology , tumor necrosis factor alpha , gene expression , transcription factor , signal transduction , gene , endocrinology , genetics
Recent evidence suggests that protein encoded by the RNA Binding Motif 10 (RBM10) gene has the ability to modulate apoptosis. The objective of this study was to test this hypothesis by manipulating RBM10 expression levels and examining the downstream consequences. The results showed that transient overexpression of RBM10 correlated with significantly elevated levels of tumour necrosis factor alpha (TNF-α) mRNA and soluble TNF-α (sTNF-α) protein, and increased apoptosis (phosphatidyl serine exposure on the outer cell membrane and nuclear condensation). Stable RNA interference-mediated RBM10 knockdown clones were less susceptible to TNF-α-mediated apoptosis, and had decreased sTNF-α protein levels. Elevated levels of TNF-α associated with RBM10 overexpression resulted from increased TNF-α transcription, not TNF-α mRNA stabilization. These results suggest that RBM10 has the ability to modulate apoptosis, and that it does so via a mechanism involving alterations to TNFR super family-mediated signaling. These data provide the first direct evidence that human RBM10 can function as an apoptosis modulator and cytokine expression regulator.

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